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A towering genome: Experimentally validated adaptations to high blood pressure and extreme stature in the giraffe

The suite of adaptations associated with the extreme stature of the giraffe has long interested biologists and physiologists. By generating a high-quality chromosome-level giraffe genome and a comprehensive comparison with other ruminant genomes, we identified a robust catalog of giraffe-specific mu...

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Detalles Bibliográficos
Autores principales: Liu, Chang, Gao, Jianbo, Cui, Xinxin, Li, Zhipeng, Chen, Lei, Yuan, Yuan, Zhang, Yaolei, Mei, Liangwei, Zhao, Lan, Cai, Dan, Hu, Mingliang, Zhou, Botong, Li, Zihe, Qin, Tao, Si, Huazhe, Li, Guangyu, Lin, Zeshan, Xu, Yicheng, Zhu, Chenglong, Yin, Yuan, Zhang, Chenzhou, Xu, Wenjie, Li, Qingjie, Wang, Kun, Gilbert, M. Thomas P., Heller, Rasmus, Wang, Wen, Huang, Jinghui, Qiu, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968835/
https://www.ncbi.nlm.nih.gov/pubmed/33731352
http://dx.doi.org/10.1126/sciadv.abe9459
Descripción
Sumario:The suite of adaptations associated with the extreme stature of the giraffe has long interested biologists and physiologists. By generating a high-quality chromosome-level giraffe genome and a comprehensive comparison with other ruminant genomes, we identified a robust catalog of giraffe-specific mutations. These are primarily related to cardiovascular, bone growth, vision, hearing, and circadian functions. Among them, the giraffe FGFRL1 gene is an outlier with seven unique amino acid substitutions not found in any other ruminant. Gene-edited mice with the giraffe-type FGFRL1 show exceptional hypertension resistance and higher bone mineral density, both of which are tightly connected with giraffe adaptations to high stature. Our results facilitate a deeper understanding of the molecular mechanism underpinning distinct giraffe traits, and may provide insights into the study of hypertension in humans.